Product Recalls in Indiana

Product recalls affecting Indiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Indiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,967 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
1,967 in last 12 months

Showing 2056120580 of 29,228 recalls

Medical DeviceJune 6, 2016· Stryker Neurovascular

Recalled Item: Target Detachable Coils: TARGET HELICAL NANO 3MM X 8CM MODEL Recalled by...

The Issue: Stryker Neurovascular has become aware that some units of Target Nano...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2016· Stryker Neurovascular

Recalled Item: Target Detachable Coils: TARGET 360 NANO 3MM X 6CM MODEL Recalled by Stryker...

The Issue: Stryker Neurovascular has become aware that some units of Target Nano...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2016· Stryker Neurovascular

Recalled Item: Target Detachable Coils: TARGET HELICAL NANO 1.5 MM X 4 Recalled by Stryker...

The Issue: Stryker Neurovascular has become aware that some units of Target Nano...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2016· Stryker Neurovascular

Recalled Item: Target Detachable Coils: TARGET 360 NANO 1 MM X 2 Recalled by Stryker...

The Issue: Stryker Neurovascular has become aware that some units of Target Nano...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2016· Stryker Neurovascular

Recalled Item: Target Detachable Coils: TARGET HELICAL NANO 3MM X 4CM MODEL Recalled by...

The Issue: Stryker Neurovascular has become aware that some units of Target Nano...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Trident Constrained Liner Inserter/Impactor Tip...

The Issue: Impactors do not meet the required sterility assurance level (SAL) of 10-6...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2016· Parker Medical

Recalled Item: Parker Trach-Vac Endotracheal Tubes. Tyvek pouches Recalled by Parker...

The Issue: Parker Medical announces a voluntary field action for the Parker Trach-Vac...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2016· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS Immunodiagnostic Products Total T4 Reagent Pack Recalled by...

The Issue: Ortho-Clinical Diagnostics confirmed that sample results generated from...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2016· Arrow International Inc

Recalled Item: ARROW Recalled by Arrow International Inc Due to Arrow is recalling these...

The Issue: Arrow is recalling these products due to the possibility that although the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2016· BBI SOLUTIONS OEM LTD

Recalled Item: SimpliRED D-Dimer Recalled by BBI SOLUTIONS OEM LTD Due to A component of...

The Issue: A component of the kit is showing a sensitivity performance detected in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Pentax of America Inc

Recalled Item: Pentax Video Bronchoscope Designed to be used with a Pentax Recalled by...

The Issue: Pentax America Inc. is recalling various bronchoscopes which contain an...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part # 313.232 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part # SD313.011 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Pentax of America Inc

Recalled Item: Ultrasound Video Bronchoscope The EB-1970UK Recalled by Pentax of America...

The Issue: The EB-1970UK Ultrasound Video Bronchoscope shipped between the clearance...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part #313.231 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes is...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part #313.221 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes is...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part # 313.211 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part # 313.250 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part #311.039 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes is...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part # 313.212 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing